In this article we discuss confinement of electrons in graphene via smooth magnetic fields which are finite everywhere on the plane. We shall consider two types of magnetic fields leading to systems which are conditionally exactly solvable and quasi exactly solvable. The bound state energies and wave functions in both cases have been found exactly.
In graphene moire superlattices, electronic interactions between layers are mostly hidden as band structures get crowded because of folding, making their interpretation cumbersome. Here, the evolution of the electronic band structure as a function of
the interlayer rotation angle is studied using Density Functional Theory followed by unfolding bands and then comparing them to their corresponding individual components. We observe interactions at regions not theoretically elucidated so far, where for small interlayer angles, gaps turn into discrete-like states that are evenly spaced in energy. We find that $V_{ppsigma}$ attractive interactions between out-of-plane orbitals from different layers are responsible for the discretization. Furthermore, when the interlayer angle becomes small, these discrete evenly-spaced states have energy differences comparable to graphene phonons. Thus, they might be relevant to explain electron-phonon-assisted effects, which have been experimentally observed in graphene moire superlattices.
We theoretically analyse the possibility to electrostatically confine electrons in circular quantum dot arrays, impressed on contacted graphene nanoribbons by top gates. Utilising exact numerical techniques, we compute the scattering efficiency of a
single dot and demonstrate that for small-sized scatterers the cross-sections are dominated by quantum effects, where resonant scattering leads to a series of quasi-bound dot states. Calculating the conductance and the local density of states for quantum dot superlattices we show that the resonant carrier transport through such graphene-based nanostructures can be easily tuned by varying the gate voltage.
We demonstrate that the electronic spectrum of graphene in a one-dimensional periodic potential will develop a Landau level spectrum when the potential magnitude varies slowly in space. The effect is related to extra Dirac points generated by the pot
ential whose positions are sensitive to its magnitude. We develop an effective theory that exploits a chiral symmetry in the Dirac Hamiltonian description with a superlattice potential, to show that the low energy theory contains an effective magnetic field. Numerical diagonalization of the Dirac equation confirms the presence of Landau levels. Possible consequences for transport are discussed.
We carry out an explicit calculation of the vacuum polarization tensor for an effective low-energy model of monolayer graphene in the presence of a weak magnetic field of intensity $B$ perpendicularly aligned to the membrane. By expanding the quasipa
rticle propagator in the Schwinger proper time representation up to order $(eB)^2$, where $e$ is the unit charge, we find an explicitly transverse tensor, consistent with gauge invariance. Furthermore, assuming that graphene is radiated with monochromatic light of frequency $omega$ along the external field direction, from the modified Maxwells equations we derive the intensity of transmitted light and the angle of polarization rotation in terms of the longitudinal ($sigma_{xx}$) and transverse ($sigma_{xy}$) conductivities. Corrections to these quantities, both calculated and measured, are of order $(eB)^2/omega^4$. Our findings generalize and complement previously known results reported in literature regarding the light absorption problem in graphene from the experimental and theoretical points of view, with and without external magnetic fields.
We consider confinement of Dirac fermions in $AB$-stacked bilayer graphene by inhomogeneous on-site interactions, (pseudo-)magnetic field or inter-layer interaction. Working within the framework of four-band approximation, we focus on the systems whe
re the stationary equation is reducible into two stationary equations with $2times2$ Dirac-type Hamiltonians and auxiliary interactions. We show that it is possible to find localized states by solving an effective Schrodinger equation with energy-dependent potential. We consider several scenarios where bilayer graphene is subject to inhomogneous (pseudo-)magnetic field, on-site interactions or inter-layer coupling. In explicit examples, we provide analytical solutions for the states localized by local fluctuations or periodicity defects of the interactions.